HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914606Generated: November 3, 2026
4'-Hydroxyacetophenone → HCID 28096015, compound
https://huagongshe.com/reaction/1914606
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 43578842 | HCID 43578842 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 28096015 | HCID 28096015 | 84.4% |
Reaction Steps
To a solution of 2-(2-chloroacetamido)-N-methylbenzamide 22.65 g (0.1 mol) and p-hydroxyacetophenone 16.32 g (0.12 mol) in 200 mL of butanone was added 27.60 g (0.2 mol) potassium carbonate. The mixture was stirred and heated to reflux for 4-5 hours, and monitored by TLC until the reaction was over, the reaction mixture was concentrated under reduced pressure and extracted with 300 mL of ethyl acetate to separate the organic phase, the organic phase was washed with 50 ml of 5% sodium hydroxide aqueous solution and 50 ml of brine successively, dried via anhydrous magnesium sulfate and evaporated, and the residual was purified via silica gel column chromatography to obtain 27.50 g 2-(2-(4-acetylphenoxy)acetamido)-N-methylbenzamide as white solid with yield of 84.4%, m.p. 252-253° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08614214B2 |
|---|
| Source dataset | uspto-grants-2013_12 |
|---|
| ORD ID | ord-4f4f053f951b47d181655c645b146c92 |
|---|
| Source note | uspto-grants-2013_12 |
|---|